Device recall
Z-0073-2012: Mizuho OSI Modular Table System; Product Usage: For use in orthopaedic surgery…
FDA device recall · Class I · Mizuho Orthopedic Systems Inc
Key facts
| Recall number (Z-number) | Z-0073-2012 |
|---|---|
| Recall event | 59536 |
| Product | Mizuho OSI Modular Table System; Product Usage: For use in orthopaedic surgery to provide support to a patient. |
| Product code | JEA |
| Recalling firm | Mizuho Orthopedic Systems Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 27, 2013 |
| 510(k) numbers | K910736 |
| FEI number | 2921578 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database